Evidence map›Paper›PMID 39145778›Full record

ArticleOsteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA2024

Fracture risk assessment in the presence of competing risk of death.

Thach S Tran, Dana Bliuc, Robert D Blank, Jacqueline R Center, Tuan V Nguyen

Abstract read
In one paragraph

Article in Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Thach S TranSchool of Biomedical Engineering, University of Technology Sydney, Level 10, Building 11, City Campus, Broadway, NSW, 2007, Australia. SonThach.Tran@uts.edu.au.ORCID http://orcid.org/0000-0002-6454-124X
Dana BliucGarvan Institute of Medical Research, Sydney, NSW, Australia.
Robert D BlankGarvan Institute of Medical Research, Sydney, NSW, Australia.
Jacqueline R CenterGarvan Institute of Medical Research, Sydney, NSW, Australia.
Tuan V NguyenSchool of Biomedical Engineering, University of Technology Sydney, Level 10, Building 11, City Campus, Broadway, NSW, 2007, Australia.

Funding

National Health and Medical Research Council in Australia 1195305National Health Medical Research Council Australia 1008219National Health Medical Research Council Australia 1070187National Health Medical Research Council Australia 1073430
6 · The paper itself

Abstract

purposeTo identify the optimal statistical approach for predicting the risk of fragility fractures in the presence of competing event of death.

methodsWe used real-world data from the Dubbo Osteoporosis Epidemiology Study that has monitored 3035 elderly participants for bone health and mortality. Fragility fractures were ascertained radiologically. Mortality was confirmed by the State Registry. We considered four statistical models for predicting fracture risk: (i) conventional Cox's proportional hazard model, (ii) cause-specific model, (iii) Fine-Gray sub-distribution model, and (iv) multistate model. These models were fitted and validated in the development (60% of the original sample) and validation (40%) subsets, respectively. The model performance was assessed by discrimination and calibration analyses.

resultsDuring a median follow-up of 11.3 years (IQR: 7.2, 16.2), 628 individuals (34.5%) in the development cohort fractured, and 630 (34.6%) died without a fracture. Neither the discrimination nor the 5-year prediction performance was significantly different among the models, though the conventional model tended to overestimate fracture risk (calibration-in-the-large index =  - 0.24; 95% CI: - 0.43, - 0.06). For 10-year risk prediction, the multistate model (calibration-in-the-large index =  - 0.05; 95% CI: - 0.20, 0.10) outperformed the cause-specific (- 0.23; - 0.30, - 0.08), Fine-Gray (- 0.31; - 0.46, - 0.16), and conventional model (- 0.54; - 0.70, - 0.39) which significantly overestimated fracture risk.

conclusionAdjustment for competing risk of death has minimum impact on the short-term prediction of fracture. However, the multistate model yields the most accurate prediction of long-term fracture risk and should be considered for predictive research in the elderly, who are also at high mortality risk. Fracture risk assessment might be compromised by the competing event of death. This study, using real-world data found a multistate model was superior to the current competing risk methods in fracture risk assessment. A multistate model is considered an optimal statistical method for predictive research in the elderly.

Indexed as

Osteoporotic FracturesAgedAged, 80 and overCause of DeathFemaleFollow-Up StudiesHumansMaleMiddle AgedModels, StatisticalOsteoporosisProportional Hazards ModelsRisk AssessmentCause-specificCompeting riskDeathFine-Gray sub-distributionFractureMultistate

Identifiers

PMID39145778
PMCPMC11499430

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LicenceCC BY-NC
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.